SPHINGOLIPIDOSIS PANEL 1
Sphingolipidoses are a class of lipid storage disorders relating to sphingolipid metabolism. They are generally inherited in an autosomal recessive fashion, but notably Fabry disease is X-linked recessive.Taken together, sphingolipidoses have an incidence of approximately 1 in 10000, but substantially more in certain populations such as Ashkenazi Jews.
Parameter(s) covered : 6
Report Frequency: Sample Daily by 4 pm; Report 4 days
Special Instruction: Give brief clinical history.
Price : ₹ 9400.00
Parameters
- Arylsulphatase A
- Beta Galactosidase
- Beta Glucocerebrosidase
- Profile Heading
- Sphingomyelinase
- Total Hexosaminidase